Trisomy 13 was first described as the cause of a distinct clinical syndrome in 1960 by Dr. Patau et al.[1] The clinical syndrome was initially characterized as "cerebral defects, apparent anophthalmia, cleft palate, hare lip, simian creases, trigger thumbs, polydactyly, and capillary hemangiomata."[2]
Patau syndrome is diagnosed either prenatally or at birth.[1] Advanced maternal age is a risk for Trisomy 13 due to an increased frequency of nondisjunction.[1] However, 20% of Patau syndrome can result from an unbalanced translocation and rarely by mosaicism.[1][3] Multiple large studies have detailed a poor prognosis of patients with Patau syndrome. Median survival is 7 to 10 days in live-born patients, and 90% live for less than 1 year.[1][4] Recently, there have been reports of several cases of longer survival due to aggressive medical.[4] Long surviving patients with Patau syndrome are less likely to have cerebral and cardiovascular malformations, typically the primary cause of the poor prognosis with Patau syndrome.[1][4] Even in these cases of increased survival, severe disability remains the expectation of these patients.[4]
The cause of Patau syndrome is the presence of three copies of chromosome 13; this is due most commonly to nondisjunction in meiosis, occurring more frequently in mothers of advanced age (age greater than 35).[1] Another cause is an unbalanced Robertsonian translocation, which results in two normal copies of chromosome 13 and an additional long arm of chromosome 13.[1] Another less common cause is mosaicism, which results in 3 copies of chromosome 13 in some cells and two copies in the others. Mosaicism is the outcome of a mitotic nondisjunction error and is unrelated to maternal age.[3] Prognosis is better in patients with mosaicism and patients with unbalanced translocations.[4]
Cytogenetic abnormalities are present in 50% of fetal deaths before 20 weeks gestational age and are present in 6 to 13% of stillbirths. Overall, fetal death occurs in 15% of pregnancies that are recognized clinically. Trisomy 13 is one of the more common trisomies and occurs in 1 per 5000 total births.[5] This frequency is less common than Down syndrome, which occurs in 1 per 700 total births. The incidence of Edwards syndrome is similar, occurring in about 1 per 5000 live births.
An extra copy of chromosome 13 causes the defects in Patau syndrome. Advanced maternal age is a risk factor for this pathology because of the increased frequency of nondisjunction in meiosis.[1] This extra copy of chromosome 13 disrupts normal embryonic development and leads to multiple defects.
Infants with Patau syndrome typically have intrauterine growth restriction and microcephaly. Facial defects are primarily midline and include cyclopia, cleft lip, and cleft palate. Facial features include a sloping forehead, small malformed ears, anophthalmia or microphthalmia, micrognathia, and pre-auricular tags. Central nervous system abnormalities are also usually midline, with alobar holoprosencephaly being the most common defect. Common extremity defects include postaxial polydactyly, congenital talipes equinovarus, or rocker-bottom feet.[6][3]
The spectrum of cardiac disease in Patau syndrome includes a ventricular septal defect, atrial septal defect, tetralogy of Fallot, atrioventricular septal defect, and double outlet right ventricle. Interestingly, the cardiac defects are alone typically lethal in infancy or childhood, even if left untreated.[1]
Additional organ systems affected by abnormalities include the lungs, liver, kidneys, genitourinary tract, digestive tract, and pancreas.[6] Defects in these organ systems that occur in greater than 50% of patients with Patau syndrome include cryptorchidism, hypospadias, labia minora hypoplasia, and bicornuate uterus. Abnormalities in these organ systems occurring in less than 50% of patients with Patau syndrome include omphalocele, incomplete rotation of the colon, Meckel diverticulum, polycystic kidney, hydronephrosis, and horseshoe kidney.[3]
Patients surviving past infancy have a severe psychomotor disorder, failure to thrive, mental retardation, and seizures.[7]
Diagnosis of Patau syndrome can be made prenatally with chorionic villi sampling, amniocentesis or fetal free DNA analysis.[1] These methods of testing detect trisomy 13. Prenatal ultrasound can also help detect the malformations of Patau syndrome, such as holoprosencephaly or other central nervous system anomalies, facial anomalies, skeletal abnormalities, renal or cardiac defects, and growth restriction that typically present.[8][9] Prenatal ultrasound after 17 weeks gestation is most sensitive in detecting the abnormalities of Patau syndrome.[9] Abnormal findings should have confirmation performed with a cytogenetic evaluation of fetal cells.
Tissue microarray has increased the ability to diagnose genetic alterations in fetal death, especially when the fetus is macerated.[10]
Intensive treatment of Patau syndrome is controversial due to the universally poor prognosis of patients despite treatment.[7]
At delivery, infants diagnosed with Patau syndrome may need post delivery oxygenation and ventilation; this may require intubation or tracheostomy due to facial defects. Patients with cardiac defects may require cardiac surgery to repair common cardiac abnormalities. Other surgeries may be indicated for common defects including herniorrhaphy, cleft lip repair, feeding tube placement, or corrective orthopedic surgeries.[7]
Additional treatments may be performed including specialized dietary feeds, seizure prophylaxis, prophylactic antibiotics for urinary tract infections, and the use of hearing aids.[4]
Despite aggressive management, median survival only extends to 733 days in the most recent cohorts of patients.[7]
The sonographic findings of a fetus with Patau syndrome may have overlap with Edwards syndrome (trisomy 18), Down syndrome (trisomy 21), or other chromosomal abnormalities.[8][9] Cytogenetic evaluation with chorionic villi sampling, amniocentesis, fetal free DNA analysis, or tissue microarray would distinguish trisomy 13 from these other cytogenetic abnormalities.[1]
Multiple large studies have detailed the overall poor prognosis of patients with Patau syndrome. Historically, median survival is 7 to 10 days in live-born patients, and 90% do not survive to 1 year.[1][4] Recently, reported cases of longer duration survival have come to light with the use of aggressive medical interventions.[4] Prognosis is better in patients with mosaic Patau syndrome and patients with unbalanced translocations.[4] Aggressive management with surgical and medical intervention may extend median survival to 733 days according to a recent study.[7]
Patau syndrome is caused most commonly by Trisomy 13 due to nondisjunction, an unbalanced translocation, or mosaicism.[3]
Prognosis of this disorder is poor, with a median survival of 7to 10 days without intervention. Aggressive intervention may prolong the median survival, but Patau syndrome typically has a universally poor prognosis.[7]
The distinctive abnormalities for this disorder are midline facial defects, midline CNS defects, heart defects, polydactyly, and failure to thrive.[1]
Trisomies and cytogenetic defects are more common in advanced maternal age (age greater than 35), patients considering pregnancy at this age should be counseled on this increased risk.[1]
If a fetus or newborn is diagnosed with Patau syndrome, the family should receive counseling regarding the poor prognosis of the disorder.[7]
Intensive treatment of Patau syndrome is controversial because of the universally poor prognosis even with treatment, but aggressive surgical and medical therapy can extend median life from 7 to 10 days to a reported 733 days.[7]
Trisomies and other cytogenetic abnormalities are more common with females of advanced maternal age.[1] Patients considering getting pregnant at this age should be counseled on this increased risk. If a fetus or newborn is diagnosed with Patau syndrome, the family should be counseled on the poor prognosis of the disorder.[7]
[1] | Wyllie JP,Wright MJ,Burn J,Hunter S, Natural history of trisomy 13. Archives of disease in childhood. 1994 Oct; [PubMed PMID: 7979530] |
[2] | PATAU K,SMITH DW,THERMAN E,INHORN SL,WAGNER HP, Multiple congenital anomaly caused by an extra autosome. Lancet (London, England). 1960 Apr 9; [PubMed PMID: 14430807] |
[3] | Petry P,Polli JB,Mattos VF,Rosa RC,Zen PR,Graziadio C,Paskulin GA,Rosa RF, Clinical features and prognosis of a sample of patients with trisomy 13 (Patau syndrome) from Brazil. American journal of medical genetics. Part A. 2013 Jun; [PubMed PMID: 23613355] |
[4] | Peroos S,Forsythe E,Pugh JH,Arthur-Farraj P,Hodes D, Longevity and Patau syndrome: what determines survival? BMJ case reports. 2012 Dec 6; [PubMed PMID: 23220825] |
[5] | Springett A,Wellesley D,Greenlees R,Loane M,Addor MC,Arriola L,Bergman J,Cavero-Carbonell C,Csaky-Szunyogh M,Draper ES,Garne E,Gatt M,Haeusler M,Khoshnood B,Klungsoyr K,Lynch C,Dias CM,McDonnell R,Nelen V,O'Mahony M,Pierini A,Queisser-Luft A,Rankin J,Rissmann A,Rounding C,Stoianova S,Tuckerz D,Zymak-Zakutnia N,Morris JK, Congenital anomalies associated with trisomy 18 or trisomy 13: A registry-based study in 16 European countries, 2000-2011. American journal of medical genetics. Part A. 2015 Dec; [PubMed PMID: 26347425] |
[6] | Trisomies., Levy PA,Marion R,, Pediatrics in review, 2018 Feb [PubMed PMID: 29437136] |
[7] | Tsukada K,Imataka G,Suzumura H,Arisaka O, Better prognosis in newborns with trisomy 13 who received intensive treatments: a retrospective study of 16 patients. Cell biochemistry and biophysics. 2012 Jul; [PubMed PMID: 22487910] |
[8] | Lehman CD,Nyberg DA,Winter TC 3rd,Kapur RP,Resta RG,Luthy DA, Trisomy 13 syndrome: prenatal US findings in a review of 33 cases. Radiology. 1995 Jan; [PubMed PMID: 7997556] |
[9] | Watson WJ,Miller RC,Wax JR,Hansen WF,Yamamura Y,Polzin WJ, Sonographic detection of trisomy 13 in the first and second trimesters of pregnancy. Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 2007 Sep; [PubMed PMID: 17715315] |
[10] | Reddy UM,Page GP,Saade GR, The role of DNA microarrays in the evaluation of fetal death. Prenatal diagnosis. 2012 Apr; [PubMed PMID: 22467168] |